pallidol (Q6634710)

inferred from InChIKey

chemical structure

Pallidol.svg
229 × 165; 9 KB

0 references

mass

454.141638 dalton

1 reference

(4bS,5R,9bS,10R)-5,10-bis(4-hydroxyphenyl)-4b,5,9b,10-tetrahydroindeno[2,1-a]indene-1,3,6,8-tetrol

Pallidol (English)

8 October 2016

2 references

inferred from InChIKey

5beta,10beta-Bis(4-hydroxyphenyl)-4bbeta,5,9bbeta,10-tetrahydroindeno[2,1-a]indene-1,3,6,8-tetraol

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₈H₂₂O₆

1 reference

Pallidol (English)

8 October 2016

C1=CC(=CC=C1C2C3C(C(C4=C(C=C(C=C34)O)O)C5=CC=C(C=C5)O)C6=CC(=CC(=C26)O)O)O

1 reference

Pallidol (English)

8 October 2016

C1=CC(=CC=C1[C@H]2[C@H]3[C@H]([C@@H](C4=C(C=C(C=C34)O)O)C5=CC=C(C=C5)O)C6=CC(=CC(=C26)O)O)O

1 reference

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Pallidol (English)

8 October 2016

1 reference

Cyphostemma crotalarioides

5 references

Antifungal activity of resveratrol oligomers fromCyphostemma crotalarioides

Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae)

Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae)

Cis ε-viniferin: A New Antifungal Resveratrol Dehydrodimer from Cyphostemma crotalarioides Roots

Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae)

Caragana brevifolia

1 reference

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Caragana korshinskii

1 reference

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Caragana leucophloea

1 reference

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Caragana sinica

5 references

Three Stilbene Tetramers from the Roots of Caragana sinica

Determination of hypaphorine and oligomeric stilbenes in the root of Caragana sinica by capillary electrophoresis with electrochemical detection

Five novel oligostilbenes from the roots of Caragana sinica

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Antioxidative oligostilbenes from Caragana sinica

Caragana stenophylla

1 reference

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Cyperus longus

2 references

Structures and Radical Scavenging Activities of Novel Norstilbene Dimer, Longusone A, and New Stilbene Dimers, Longusols A, B, and C, from Egyptian Herbal Medicine Cyperus longus

Structures of novel norstilbene dimer, longusone A, and three new stilbene dimers, longusols A, B, and C, with antiallergic and radical scavenging activities from Egyptian natural medicine Cyperus longus.

Mallotus pallidus

1 reference

Phloroglucinol derivatives from Mallotus pallidus

Parthenocissus tricuspidata

3 references

A resveratrol dimer from Parthenocissus tricuspidata

A resveratrol dimer from Parthenocissus tricuspidata

Two new antioxidant stilbene dimers, parthenostilbenins A and B from Parthenocissus tricuspidata

Sophora alopecuroides

2 references

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

Chemical constituents isolated from the Mongolian medicinal plant Sophora alopecuroides L. and their inhibitory effects on LPS-induced nitric oxide production in RAW 264.7 macrophages

Sophora leachiana

3 references

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

Two Novel Resveratrol Trimers, Leachianols A and B, from Sophora leachiana.

Two Novel Resveratrol Trimers, Leachianols A and B, from Sophora leachiana.

Carex

1 reference

Resveratrol oligomers isolated from Carex species inhibit growth of human colon tumorigenic cells mediated by cell cycle arrest

Carex folliculata

1 reference

Identification and bioactivities of resveratrol oligomers and flavonoids from Carex folliculata seeds

Carex unciniiformis

1 reference

Nepalensinols D-G, new resveratrol oligomers from Kobresia nepalensis (Cyperaceae) as potent inhibitors of DNA topoisomerase II.

Cissus repanda

1 reference

Pallidol, a resveratrol dimer from Cissus pallida

Rheum

1 reference

New resveratrol oligomer derivatives from the roots of Rheum lhasaense

Vitis vinifera

4 references

Two new stilbene dimer glucosides from grape (Vitis vinifera) cell cultures.

First symmetrical bicyclo[6.6.0]tetradecane resveratrol tetramer from stalks of vitis vinifera (Vitaceae)

Resveratrol and Its Oligomers from Wine Grapes Are Selective 1O2 Quenchers: Mechanistic Implication by High-Performance Liquid Chromatography−Electrospray Ionization−Tandem Mass Spectrometry and Theoretical Calculation

Direct liquid chromatographic analysis of resveratrol derivatives and flavanonols in wines with absorbance and fluorescence detection

Cissus petiolata

1 reference

Pallidol, a resveratrol dimer from Cissus pallida

Identifiers

InChI

InChI=1S/C28H22O6/c29-15-5-1-13(2-6-15)23-25-19(9-17(31)11-21(25)33)28-24(14-3-7-16(30)8-4-14)26-20(27(23)28)10-18(32)12-22(26)34/h1-12,23-24,27-34H/t23-,24-,27+,28+/m1/s1

1 reference

Pallidol (English)

8 October 2016

2 references

imported from Wikimedia project

Pallidol (English)

8 October 2016

ChEBI release 2020-09-01

CAS Registry Number

105037-88-5

1 reference

1 reference

English

title

(4bR,5R,9bR,10R)-5,10-Bis(4-hydroxyphenyl)-4b,5,9b,10-tetrahydroindeno[2,1-a]indene-1,3,6,8-tetrol (English)

8 October 2016

2 references

English

title

Pallidol (English)

retrieved

8 October 2016

Reaxys registry number

7152851

1 reference

pallidol (English)

8 October 2016

mapping relation type

2 references

English

title

pallidol (English)

retrieved

8 October 2016

International Chemical Identifier

InChI

InChI=1S/C28H22O6/c29-15-5-1-13(2-6-15)23-25-19(9-17(31)11-21(25)33)28-24(14-3-7-16(30)8-4-14)26-20(27(23)28)10-18(32)12-22(26)34/h1-12,23-24,27-34H/t23-,24-,27+,28+/m1/s1

1 reference

PALLIDOL (English)

8 October 2016

2 references

inferred from InChIKey

1 reference

1 reference

DSSTOX compound identifier

DTXCID30677749

0 references

UNII

QE5TL72TJ8

1 reference